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一套用于检测所有已知禽副粘病毒的逆转录聚合酶链反应检测方法及其在中国禽副粘病毒监测中的应用。

A set of RT-PCR assays for detection of all known avian paramyxoviruses and application in surveillance of avian paramyxoviruses in China.

作者信息

Jin Ji-Hui, Wang Jing-Jing, Ren Ying-Chao, Liu Shuo, Li Jin-Ping, Hou Guang-Yu, Liu Hua-Lei, Zhuang Qing-Ye, Wang Su-Chun, Jiang Wen-Ming, Yu Xiao-Hui, Yu Jian-Min, Yuan Li-Ping, Peng Cheng, Zhang Guo-Zhong, Chen Ji-Ming

机构信息

Laboratory for Avian Disease Surveillance (OIE Reference Laboratory for Newcastle Disease), China Animal Health and Epidemiology Center, Qingdao, China.

Department for Animal Health Assessment, China Animal Health and Epidemiology Center, Qingdao, China.

出版信息

PeerJ. 2021 Mar 4;9:e10748. doi: 10.7717/peerj.10748. eCollection 2021.

Abstract

BACKGROUND

Avian paramyxoviruses (APMVs), also termed avian avulaviruses, are of a vast diversity and great significance in poultry. Detection of all known APMVs is challenging, and distribution of APMVs have not been well investigated.

METHODS

A set of reverse transcription polymerase chain reaction (RT-PCR) assays for detection of all known APMVs were established using degenerate primers targeting the viral polymerase L gene. The assays were preliminarily evaluated using in-vitro transcribed double-stranded RNA controls and 24 known viruses, and then they were employed to detect 4,346 avian samples collected from 11 provinces.

RESULTS

The assays could detect 20-200 copies of the double-stranded RNA controls, and detected correctly the 24 known viruses. Of the 4,346 avian samples detected using the assays, 72 samples were found positive. Of the 72 positives, 70 were confirmed through sequencing, indicating the assays were specific for APMVs. The 4,346 samples were also detected using a reported RT-PCR assay, and the results showed this RT-PCR assay was less sensitive than the assays reported here. Of the 70 confirmed positives, 40 were class I Newcastle disease virus (NDV or APMV-1) and 27 were class II NDV from poultry including chickens, ducks, geese, and pigeons, and three were APMV-2 from parrots. The surveillance identified APMV-2 in parrots for the first time, and revealed that prevalence of NDVs in live poultry markets was higher than that in poultry farms. The surveillance also suggested that class I NDVs in chickens could be as prevalent as in ducks, and class II NDVs in ducks could be more prevalent than in chickens, and class II NDVs could be more prevalent than class I NDVs in ducks. Altogether, we developed a set of specific and sensitive RT-PCR assays for detection of all known APMVs, and conducted a large-scale surveillance using the assays which shed novel insights into APMV epidemiology.

摘要

背景

禽副粘病毒(APMVs),也称为禽正粘病毒,种类繁多,在家禽中具有重要意义。检测所有已知的APMVs具有挑战性,且其分布情况尚未得到充分研究。

方法

使用针对病毒聚合酶L基因的简并引物,建立了一套用于检测所有已知APMVs的逆转录聚合酶链反应(RT-PCR)检测方法。使用体外转录的双链RNA对照和24种已知病毒对这些检测方法进行了初步评估,然后用于检测从11个省份收集的4346份禽类样本。

结果

这些检测方法能够检测到20 - 200拷贝的双链RNA对照,并正确检测出24种已知病毒。在使用这些检测方法检测的4346份禽类样本中,有72份样本呈阳性。在这72份阳性样本中,70份通过测序得到确认,表明这些检测方法对APMVs具有特异性。还使用一种已报道的RT-PCR检测方法对这4346份样本进行了检测,结果表明该RT-PCR检测方法的灵敏度低于本文报道的检测方法。在70份经确认的阳性样本中,40份为I类新城疫病毒(NDV或APMV-1),27份为来自鸡、鸭、鹅和鸽子等家禽的II类NDV,3份为来自鹦鹉的APMV-2。此次监测首次在鹦鹉中发现了APMV-2,并揭示了活禽市场中NDVs的流行率高于家禽养殖场。监测还表明,鸡中的I类NDVs流行率与鸭中的相当,鸭中的II类NDVs流行率可能高于鸡中的,且鸭中的II类NDVs流行率可能高于I类NDVs。总之,我们开发了一套用于检测所有已知APMVs的特异性和灵敏性RT-PCR检测方法,并使用这些检测方法进行了大规模监测,为APMVs流行病学提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fd/7937338/7379a1b34e43/peerj-09-10748-g001.jpg

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